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9.1.1 Congenital glaucoma, Buphthalmos (97)
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Display all abstracts in classification 9.1.1 Congenital glaucoma, Buphthalmos
Search within classification 9.1.1 Congenital glaucoma, Buphthalmos61040 Neural crest derivatives in ocular development: Discerning the eye of the storm
Williams AL
Birth Defects Research Part C-Embryo Today: Reviews 2015; 105: 87-95
61310 Novel mutations in PAX6, OTX2 and NDP in anophthalmia, microphthalmia and coloboma
Deml B
European Journal of Human Genetics 2016; 24: 535-541
61379 Outcomes of Ahmed glaucoma valve implantation in advanced primary congenital glaucoma with previous surgical failure
Huang J
Clinical Ophthalmology 2015; 9: 977-983
61142 RETINAL AND CHOROIDAL CHANGES OF NANOPHTHALMIC EYES WITH AND WITHOUT SECONDARY GLAUCOMA
Xiao H
Retina (Philadelphia, Pa.) 2015; 35: 2121-2129
61308 Phakomatosis Pigmentovascularis Associated With Sturge-Weber Syndrome, Ota Nevus, and Congenital Glaucoma
Yang Y
Medicine 2015; 94: e1025
61560 Newborn Glaucoma with Imperforate Pupil
Mandal AK
Optometry and Vision Science 2015; 92: e380-e382
61703 CYP1B1 gene analysis and phenotypic correlation in Portuguese children with primary congenital glaucoma
Cardoso MS
European Journal of Ophthalmology 2015; 0: 0
60977 Polymorphic Variants of Cytochrome P450: Relevance to Cancer and Other Diseases
Daly AK
Advances in Pharmacology 2015; 74: 85-111
61522 Rare FOXC1 variants in congenital glaucoma: identification of translation regulatory sequences
Medina-Trillo C
European Journal of Human Genetics 2016; 24: 672-680
61587 Homozygous p.G61E mutation in a consanguineous Pakistani family with co-existence of juvenile-onset open angle glaucoma and primary congenital glaucoma
Bashir R
Gene 2015; 570: 295-298
61537 Boston type 1 keratoprosthesis for primary congenital glaucoma
Haugsdal JM
British Journal of Ophthalmology 2016; 100: 328-331
61550 PERIPHERAL RETINAL DEGENERATIONS AND RHEGMATOGENOUS DETACHMENT IN PRIMARY CONGENITAL GLAUCOMA
Gupta S
Retina (Philadelphia, Pa.) 2016; 36: 188-191
61662 Optical Coherence Tomography in an Infant with Walker-Warburg Syndrome
Mano N
Case Reports in Ophthalmology 2015; 6: 210-215
61341 A case of WAGR syndrome in association with developmental glaucoma requiring bilateral Baerveldt glaucoma implants and subsequent tube repositioning
Akagi T
Clinical Ophthalmology 2015; 9: 1081-1084
61125 Genotype-Phenotype Correlations in CYP1B1-Associated Primary Congenital Glaucoma Patients Representing Two Large Cohorts from India and Brazil
de Melo MB
PLoS ONE 2015; 10: e0127147
61558 Novel BCOR mutation in a boy with Lenz microphthalmia/oculo-facio-cardio-dental (OFCD) syndrome
Zhu X
Gene 2015; 571: 142-144
61524 Phenotypic Expansion of Congenital Disorder of Glycosylation Due to SRD5A3 Null Mutation
Tuysuz B
JIMD reports 2015; 0:
61703 CYP1B1 gene analysis and phenotypic correlation in Portuguese children with primary congenital glaucoma
Anjos R
European Journal of Ophthalmology 2015; 0: 0
61558 Novel BCOR mutation in a boy with Lenz microphthalmia/oculo-facio-cardio-dental (OFCD) syndrome
Dai FR
Gene 2015; 571: 142-144
61560 Newborn Glaucoma with Imperforate Pupil
Ramappa M
Optometry and Vision Science 2015; 92: e380-e382
61537 Boston type 1 keratoprosthesis for primary congenital glaucoma
Goins KM
British Journal of Ophthalmology 2016; 100: 328-331
61125 Genotype-Phenotype Correlations in CYP1B1-Associated Primary Congenital Glaucoma Patients Representing Two Large Cohorts from India and Brazil
Mandal AK
PLoS ONE 2015; 10: e0127147
61524 Phenotypic Expansion of Congenital Disorder of Glycosylation Due to SRD5A3 Null Mutation
Pehlivan D
JIMD reports 2015; 0:
61341 A case of WAGR syndrome in association with developmental glaucoma requiring bilateral Baerveldt glaucoma implants and subsequent tube repositioning
Yoshikawa M
Clinical Ophthalmology 2015; 9: 1081-1084
61522 Rare FOXC1 variants in congenital glaucoma: identification of translation regulatory sequences
Aroca-Aguilar JD
European Journal of Human Genetics 2016; 24: 672-680
